SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6352390 | snp | C/T | 0.5 | 0 | intron-variant | Asb18, LOC105246658 | Mm_Celera | 1:89963612 | ctccaggcccacaaa[C/T]tgttagatgaaacaa | 208372 |
rs6352866 | snp | G/T | 0.5 | 0 | intron-variant | Asb18, LOC105246658 | Mm_Celera | 1:89963676 | cacagcagataaaaa[G/T]aAAGAAATAATATGC | 208372 |
rs6352950 | snp | G/T | 0.5 | 0 | intron-variant | Asb18, LOC105246658 | Mm_Celera | 1:89963736 | ACCCTTATAAAGCCT[G/T]GTGCTTCTGTGACAT | 208372 |
rs6367234 | snp | G/T | 0.5 | 0 | intron-variant | Asb18, LOC105246658 | Mm_Celera | 1:89964042 | aagagcagtatgtgc[G/T]tctaatcTTCTAATC | 208372 |
rs6385691 | snp | C/G | 0.5 | 0 | intron-variant | Asb18, LOC105246658 | Mm_Celera | 1:89965142 | AAGTCCCTTGCAATC[C/G]TGTGGTGATCCTTGA | 208372 |
rs6386347 | snp | C/G | 0.5 | 0 | intron-variant | Asb18, LOC105246658 | Mm_Celera | 1:89965310 | ATGCACAGCCCCCCC[C/G]NCCCCCATCCTGAGG | 208372 |
rs6386348 | snp | A/C | 0.5 | 0 | intron-variant | Asb18, LOC105246658 | GRCm38.p3 | 1:89965310 | TGCACAGCCCCCCCN[A/C]CCCCCATCCTGAGGT | 208372 |
rs30338394 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb18 | Mm_Celera | 1:89979809 | TTTGGCTCTCCCATT[C/T]CATATCCATGTGATG | 208372 |
rs30338395 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Asb18 | Mm_Celera | 1:89979755 | AAACTAACATTGGTA[C/T]TCTCTGACAGACTAA | 208372 |
rs30338396 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Asb18 | Mm_Celera | 1:89979499 | TGATCTAAATGCAAA[C/T]TGTTGGCTTATTATA | 208372 |
rs30338397 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Asb18 | Mm_Celera | 1:89979385 | AGTCATACACCTTTG[C/T]GATGCTTAAAAAGCA | 208372 |
rs30338398 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Asb18 | Mm_Celera | 1:89979258 | AAGGAAAGGTCTACA[A/C]AGAGAGAAATGGAAG | 208372 |
rs30338399 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Asb18 | Mm_Celera | 1:89979052 | TAAGGTAGTGGGCTA[C/T]GTTATTGTAGAGGTG | 208372 |
rs30338400 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Asb18 | Mm_Celera | 1:89978995 | AGAAAAGCCTGGTTG[C/T]GCCCTCAAGTCCCTT | 208372 |
rs30338401 | snp | A/G | 0.5 | 0 | intron-variant | Asb18 | Mm_Celera | 1:89978894 | ATCCCAGAGAAAGTA[A/G]CTCTTTTTTTGTCAA | 208372 |
rs30338402 | snp | A/C | 0.375 | 0.216506 | intron-variant | Asb18 | Mm_Celera | 1:89978776 | AGCATTGTCAGAAGG[A/C]AGAGGAAACCAAATG | 208372 |
rs30338403 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Asb18 | Mm_Celera | 1:89978606 | CTCGTGTTCTGAATC[C/G]CGAATTCTGAAGCTT | 208372 |
rs30339344 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Asb18 | Mm_Celera | 1:89977695 | CCTGATAAAGTCCTG[A/G]GCAGAGCAGCTTTGC | 208372 |
rs30339345 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Asb18 | Mm_Celera | 1:89977527 | CTACTAAGATGCCTT[A/G]CATTCATGTTGACTG | 208372 |
rs30339346 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Asb18 | Mm_Celera | 1:89977472 | ACAGAGATCTCCAAA[C/T]AAATCAGAGTGGGGT | 208372 |
rs30339347 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb18 | Mm_Celera | 1:89977310 | GCACTACCTGCACAC[A/G]CTTGTCTGTCTTTGG | 208372 |
rs30339348 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Asb18 | Mm_Celera | 1:89977155 | ATACAGGGAGAAGCA[A/G]AAAACTGAGGACCTC | 208372 |
rs30339349 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Asb18 | Mm_Celera | 1:89975940 | AGGTTCTGTCTTGGT[C/T]TTGCACCTGTCTTTC | 208372 |
rs30339350 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Asb18 | Mm_Celera | 1:89975890 | CATCCCTGCTGCTGA[C/T]CTGATTTCTCTCAGT | 208372 |
rs30339351 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Asb18 | Mm_Celera | 1:89975731 | ATATCGAAACAAGAC[C/T]GAATACTTTTGAAGT | 208372 |
rs30339352 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Asb18 | Mm_Celera | 1:89975720 | GTGGAGAGCTGATAT[C/G]GAAACAAGACCGAAT | 208372 |
rs30339353 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Asb18 | Mm_Celera | 1:89975692 | AGCATCAGAGCGAGA[A/G]AAAAGTGGCAGGGTG | 208372 |
rs30340294 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Asb18 | Mm_Celera | 1:89975677 | AAGAGGAGAGCCAAA[A/G]GCATCAGAGCGAGAG | 208372 |
rs30340295 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Asb18 | Mm_Celera | 1:89975568 | TCTAGTGTCCTTTCT[C/T]CCAAAAAATGATAAA | 208372 |
rs30340296 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb18 | Mm_Celera | 1:89975096 | GACATAATTGAATGA[A/G]AAACAATTTGGCTCT | 208372 |
rs30340297 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Asb18 | Mm_Celera | 1:89975040 | TTTGGGGCCAACTGT[A/C]CCCTAGATTGTACAC | 208372 |
rs30340298 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Asb18 | Mm_Celera | 1:89974962 | ACCTTCGTCTCTCTC[A/G]GAGCAATGGCTACTG | 208372 |
rs30340299 | snp | A/C | 0.375 | 0.216506 | intron-variant | Asb18 | Mm_Celera | 1:89974922 | GTCAGTGGACAGAGC[A/C]TTCAGGGCAGAGGAA | 208372 |
rs30340300 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Asb18 | Mm_Celera | 1:89974737 | TTCCTGAGCCAGCTT[A/G]GCGTGAAGGACCGGA | 208372 |
rs30340301 | snp | A/G/T | 0.197531 | 0.244432 | intron-variant | Asb18 | GRCm38.p3 | 1:89974689 | AGGGAAATGTAGCCA[A/G/T]GCGGTAGAGAAAGGG | 208372 |
rs30340302 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Asb18 | Mm_Celera | 1:89974466 | TTCATGATAACCACC[A/G]TGTCCAGGATGGTGG | 208372 |
rs30340303 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb18 | Mm_Celera | 1:89974402 | CGTTACTCGCATCCC[A/G]CCGTTTAGCACAATT | 208372 |
rs30340484 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Asb18, Gm34616 | Mm_Celera | 1:90006655 | TGTGTGCTCCGCACC[A/G]CTACGGTGCTCTTTC | 208372 |
rs30340485 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Asb18, Gm34616 | Mm_Celera | 1:90006430 | CTACTTCCACCCTTC[C/T]TATGTATGGAAAAGA | 208372 |
rs30340486 | snp | A/C | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Asb18, Gm34616 | Mm_Celera | 1:90005943 | TTTCTAGCCAATGGA[A/C]TCTGCTCTTCATTAC | 208372 |
rs30340487 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Asb18, Gm34616 | Mm_Celera | 1:90004914 | GAAGGCCTCAGAGGA[C/T]GTGTGGGTTTCAGGA | 208372 |
rs30340488 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Asb18, Gm34616 | Mm_Celera | 1:90004867 | ACTTCTTGGAAGGAG[A/G]AATAGATATGCTGGT | 208372 |
rs30340489 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Asb18, Gm34616 | Mm_Celera | 1:90004697 | AGATGGCTCCAGGTA[C/G]CAGCGGGGAGATACT | 208372 |
rs30340490 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Asb18, Gm34616 | Mm_Celera | 1:90004414 | AATTGTTGTAGGGGA[C/G]CAAACCCCATTATTC | 208372 |
rs30340491 | snp | C/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Asb18, Gm34616 | Mm_Celera | 1:90003677 | AAAGAGTTTCTTAGG[C/G]AACTGAGTTTTGGAA | 208372 |
rs30340492 | snp | C/T | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Asb18, Gm34616 | Mm_Celera | 1:90003387 | ACACACCTATGCATG[C/T]GGAAAATGTAAGTTA | 208372 |
rs30340493 | snp | A/G | 0.498615 | 0.0262793 | intron-variant, upstream-variant-2KB | Asb18, Gm34616 | Mm_Celera | 1:90003047 | TTATATAAACGAAAC[A/G]AGTATCAAATACATA | 208372 |
rs30341044 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Asb18 | Mm_Celera | 1:89974385 | CCCCTTGAGTCCTTG[G/T]ACGTTACTCGCATCC | 208372 |
rs30341045 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Asb18 | Mm_Celera | 1:89974114 | CAGGCACAGGAGACA[A/C]GATGGTCAATGCAGG | 208372 |
rs30341046 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Asb18 | Mm_Celera | 1:89974047 | GGTGGACTCATTCTC[C/T]CTGGGGTGTGGCGCC | 208372 |
rs30341047 | snp | A/T | 0.5 | 0 | intron-variant | Asb18 | Mm_Celera | 1:89974014 | GAGAGAGAGAGAGAG[A/T]CCTCATTAACCCTCT | 208372 |
rs30341048 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Asb18 | Mm_Celera | 1:89972253 | TGTTTTCTGTGGAAA[A/C]TACCCAGCTGGAGAG | 208372 |
rs30341049 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb18 | Mm_Celera | 1:89971951 | ATAAGAACAGCCGAC[A/G]CCATTATCCACAGAA | 208372 |
rs30341050 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb18 | Mm_Celera | 1:89971853 | CCAGCACAGTAGGGT[A/G]CTTTGCTCACAAGGG | 208372 |
rs30341051 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Asb18 | Mm_Celera | 1:89971144 | TTTCTCTTGCCTCCA[C/T]ATCAGCAGTATCATG | 208372 |
rs30341052 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb18 | Mm_Celera | 1:89971118 | CAGTATTTTTTAATT[C/T]TCCCTTTGTGTTTCT | 208372 |
rs30341053 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Asb18 | Mm_Celera | 1:89971021 | TTTACTTAACTGGGG[C/T]TCTGATCCAGCTCAT | 208372 |
rs30341324 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Asb18, Gm34616 | Mm_Celera | 1:90002710 | AATTCCGTGTGATAC[A/G]GGGAAGATTCTTTGG | 208372 |
rs30341325 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Asb18, Gm34616 | Mm_Celera | 1:90002529 | TTGAGACAAATTGCA[C/T]GCTCAGCCTGATTGT | 208372 |
rs30341326 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Asb18, Gm34616 | GRCm38.p3 | 1:90002383 | TGGCACCAATTCTGG[C/G/T]AGGACATTTGTAGAC | 208372 |
rs30341327 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb18 | Mm_Celera | 1:90001855 | GAAGTCTGGCAGGTA[C/T]ATAAAGCTCAATTTT | 208372 |
rs30341328 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb18 | Mm_Celera | 1:90000934 | GATCTTGGTTTCCTG[C/T]GTCCGAGCTGACACA | 208372 |
rs30341329 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Asb18 | Mm_Celera | 1:90000876 | CCCCGGGTTGCACAC[A/T]TGATGGAGTTTGAGG | 208372 |
rs30341330 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Asb18 | Mm_Celera | 1:90000864 | ACATTCAGATGGCCC[A/C]GGGTTGCACACATGA | 208372 |
rs30341331 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb18 | Mm_Celera | 1:90000838 | CTCTAGATCCAGTGA[C/T]GGTGGACTCCACATT | 208372 |
rs30341332 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb18 | Mm_Celera | 1:90000195 | GGTCTGACTTTTCTT[A/G]GCTAGCATCTTGTTT | 208372 |
rs30341333 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:90000151 | GAGCTTGCGTACATC[C/T]GGTTCTGCCTCTACA | 208372 |
rs30341884 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Asb18 | Mm_Celera | 1:89970631 | ACAGTTGTGTGCCCT[C/T]ATGCCCGCGTGTGTA | 208372 |
rs30341885 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Asb18 | Mm_Celera | 1:89970523 | CCGGTGTCACCTAGA[C/G]CAGTTCCACTGGGTA | 208372 |
rs30341886 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Asb18 | Mm_Celera | 1:89970441 | CATGCAACCCAGAAA[G/T]GATCTCTGTGGTGTG | 208372 |
rs30341887 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Asb18 | Mm_Celera | 1:89970348 | TTCTCATCATTCCCA[C/T]TGTCATTGCCTTTTG | 208372 |
rs30341888 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb18 | Mm_Celera | 1:89970303 | CTGTGACTGACTAGC[C/T]TGGCCAGTGACAGTC | 208372 |
rs30341889 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Asb18 | Mm_Celera | 1:89970117 | CTCTGGAGTTTACCG[C/T]GGATCCACTGAGAGT | 208372 |
rs30341890 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb18 | Mm_Celera | 1:89969767 | ACTTCTCTTCCTCAG[A/G]CAGTGCTGTGGTAAC | 208372 |
rs30341891 | snp | G/T | 0.375 | 0.216506 | intron-variant | Asb18 | Mm_Celera | 1:89969384 | AACTGGATTCAAGAC[G/T]GCCTTTGACTCCAGA | 208372 |
rs30341892 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Asb18 | Mm_Celera | 1:89957603 | CCACATGCAGAAGAC[A/T]CTGACTGATACAGGG | 208372 |
rs30341893 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb18 | Mm_Celera | 1:89957500 | TACATGAAGCATTGT[A/G]TCAACCCTAATAACA | 208372 |
rs30342204 | snp | A/C | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:90000069 | TGGCTGTCAGAACCC[A/C]GAGTCCTTCCTGGAG | 208372 |
rs30342205 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999987 | CTGGAGTTATTTTAA[A/G]CCATCAAAGCATGTT | 208372 |
rs30342206 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999937 | CATACTGATGTTTGC[A/G]CCCAAATTTAGGTGA | 208372 |
rs30342207 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999890 | GGCTTCACTTTCTCG[A/T]TGGGTAGTTTAGAGG | 208372 |
rs30342208 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999868 | TCCTCCTGTTTATGT[C/T]TCTAGAGGCTTCACT | 208372 |
rs30342209 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999849 | CTGCTGTTCACTGTC[C/T]GGGTCCTCCTGTTTA | 208372 |
rs30342210 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999731 | CAATCGGCTCCAAAT[A/G]ATCTCAGCCAGCCAG | 208372 |
rs30342211 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999691 | ATCCATGTGAATATA[C/T]GGAGGGGAAACGGCG | 208372 |
rs30342212 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999667 | CACTGCAGGTGCTGC[C/T]TTCAGGTGATCCATG | 208372 |
rs30342213 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Asb18 | Mm_Celera | 1:89999347 | TGAGGTAAAGGGTGT[G/T]TGCACTTCAACCTGA | 208372 |
rs30342345 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Asb18 | Mm_Celera | 1:90016107 | GGTTGTCTTTGAAAG[A/G]TTTGCGGTATGTGTG | 208372 |
rs30342346 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Asb18 | Mm_Celera | 1:90015796 | TGGGTGGCTAATCAG[C/T]GGCACATGCACTATG | 208372 |
rs30342347 | snp | A/T | 0.32 | 0.24 | upstream-variant-2KB | Asb18 | Mm_Celera | 1:90015363 | TATTTACTGTTTGAT[A/T]TATAGACATGTGGTC | 208372 |
rs30342348 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Asb18 | Mm_Celera | 1:90014848 | GAGGTGACTTTGTTT[A/G]CTTGAGAGGGTTGGA | 208372 |
rs30342349 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, utr-variant-5-prime | Asb18 | Mm_Celera | 1:90014666 | CAGAGCAGGACAGAT[A/G]GCTATAAATAGAATC | 208372 |
rs30342350 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-5-prime | Asb18 | Mm_Celera | 1:90014609 | GTGCAGGGCCAGCCT[C/T]CTTCTCTTCCTCTAA | 208372 |
rs30342351 | snp | C/T | 0.32 | 0.24 | missense | Asb18 | Mm_Celera | 1:90014532 | TTAATCTCCTCACTA[C/T]GTCTGAGCTGAGGGG | 208372 |
rs30342352 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Asb18 | Mm_Celera | 1:90014431 | CCAGTCATCATTAGC[A/G]AGTTCTATTACGGCG | 208372 |
rs30342353 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb18 | Mm_Celera | 1:90013570 | GAAGTGCTTCTGTAG[A/G]TAGCCTGTCTAGTGG | 208372 |
rs30342764 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb18 | Mm_Celera | 1:89957194 | GAGGATCTCATGAAA[C/T]AGTCAGTGGTGCCAT | 208372 |
rs30342765 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb18 | Mm_Celera | 1:89957167 | TCATCACAGCAGTGT[A/G]TGTGTGTGAGTGAGG | 208372 |
rs30342766 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb18 | Mm_Celera | 1:89957137 | ATTCCACCTTGTCCT[C/T]CTTGTCTAGTCTCTT | 208372 |
rs30342767 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb18 | Mm_Celera | 1:89957089 | GCACTTCCTTAGTCC[C/T]ATGGTGTCCCTCATG | 208372 |